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Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?

Inflammasome activation is exclusively involved in sensing activation of innate immunity and inflammatory response during viral infection. Accumulating evidence suggests that the manipulation of inflammasome assembly or its interaction with viral proteins are critical factors in viral pathogenesis....

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Detalles Bibliográficos
Autores principales: Deng, Chuan-Han, Li, Tian-Qi, Zhang, Wei, Zhao, Qi, Wang, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384481/
https://www.ncbi.nlm.nih.gov/pubmed/37515138
http://dx.doi.org/10.3390/v15071451
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author Deng, Chuan-Han
Li, Tian-Qi
Zhang, Wei
Zhao, Qi
Wang, Ying
author_facet Deng, Chuan-Han
Li, Tian-Qi
Zhang, Wei
Zhao, Qi
Wang, Ying
author_sort Deng, Chuan-Han
collection PubMed
description Inflammasome activation is exclusively involved in sensing activation of innate immunity and inflammatory response during viral infection. Accumulating evidence suggests that the manipulation of inflammasome assembly or its interaction with viral proteins are critical factors in viral pathogenesis. Results from pilot clinical trials show encouraging results of NLRP3 inflammasome suppression in reducing mortality and morbidity in SARS-CoV-2-infected patients. In this article, we summarize the up-to-date understanding of inflammasomes, including NLRP3, AIM2, NLRP1, NLRP6, and NLRC4 in various viral infections, with particular focus on RNA viruses such as SARS-CoV-2, HIV, IAV, and Zika virus and DNA viruses such as herpes simplex virus 1. We also discuss the current achievement of the mechanisms involved in viral infection-induced inflammatory response, host defense, and possible therapeutic solutions.
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spelling pubmed-103844812023-07-30 Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution? Deng, Chuan-Han Li, Tian-Qi Zhang, Wei Zhao, Qi Wang, Ying Viruses Review Inflammasome activation is exclusively involved in sensing activation of innate immunity and inflammatory response during viral infection. Accumulating evidence suggests that the manipulation of inflammasome assembly or its interaction with viral proteins are critical factors in viral pathogenesis. Results from pilot clinical trials show encouraging results of NLRP3 inflammasome suppression in reducing mortality and morbidity in SARS-CoV-2-infected patients. In this article, we summarize the up-to-date understanding of inflammasomes, including NLRP3, AIM2, NLRP1, NLRP6, and NLRC4 in various viral infections, with particular focus on RNA viruses such as SARS-CoV-2, HIV, IAV, and Zika virus and DNA viruses such as herpes simplex virus 1. We also discuss the current achievement of the mechanisms involved in viral infection-induced inflammatory response, host defense, and possible therapeutic solutions. MDPI 2023-06-27 /pmc/articles/PMC10384481/ /pubmed/37515138 http://dx.doi.org/10.3390/v15071451 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Deng, Chuan-Han
Li, Tian-Qi
Zhang, Wei
Zhao, Qi
Wang, Ying
Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title_full Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title_fullStr Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title_full_unstemmed Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title_short Targeting Inflammasome Activation in Viral Infection: A Therapeutic Solution?
title_sort targeting inflammasome activation in viral infection: a therapeutic solution?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10384481/
https://www.ncbi.nlm.nih.gov/pubmed/37515138
http://dx.doi.org/10.3390/v15071451
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